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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Pieris-Pharmaceuticals-Inc-US7207951036">Pieris Pharmaceuticals, Inc.</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/03/3305944/0/en/Palvella-Therapeutics-Announces-Completion-of-FDA-Pre-NDA-Meeting-for-QTORIN-Rapamycin-in-Microcystic-Lymphatic-Malformations.html">Palvella Therapeutics Announces Completion of FDA Pre-NDA Meeting for QTORIN™ Rapamycin in Microcystic Lymphatic Malformations</a>
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        Palvella remains on track to submit an NDA in the second half of 2026 Microcystic lymphatic malformations are serious, chronic, lifelong vascular malformations that can cause persistent leaking, bleeding, infection, functional impairment, and significant daily burden for patients and families QTORIN™ rapamycin has the potential to become the first FDA-approved therapy and standard of care for t...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Pieris-Pharmaceuticals-Inc-US7207951036">Pieris Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/02/3305033/0/en/Palvella-Therapeutics-to-Participate-in-the-Goldman-Sachs-47th-Annual-Global-Healthcare-Conference-2026.html">Palvella Therapeutics to Participate in the Goldman Sachs 47th Annual Global Healthcare Conference 2026</a>
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        WAYNE, Pa., June 02, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc. (Palvella or the “Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapies to treat patients suffering from serious, rare skin diseases and vascular malformations for which there are no U.S. Food and Drug Administration (FDA)-approved therapies, today a...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Pieris-Pharmaceuticals-Inc-US7207951036">Pieris Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/27/3301826/0/en/Palvella-Therapeutics-Strengthens-QTORIN-Pitavastatin-Intellectual-Property-with-Yale-Licensed-U-S-Patent-Providing-Protection-into-2043.html">Palvella Therapeutics Strengthens QTORIN™ Pitavastatin Intellectual Property with Yale-Licensed U.S. Patent Providing Protection into 2043</a>
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        Yale-licensed U.S. patent provides broad protection for topical mevalonate pathway inhibition in porokeratosis, including disseminated superficial actinic porokeratosis (DSAP)
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/21/3299219/0/en/palvella-therapeutics-named-healthcare-life-sciences-company-of-the-year-at-the-philadelphia-alliance-for-capital-and-technologies-pact-ecosystem-awards.html">Palvella Therapeutics Named Healthcare &amp; Life Sciences Company of the Year at the Philadelphia Alliance for Capital and Technologies (PACT) Ecosystem Awards</a>
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        WAYNE, Pa., May 21, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc. (Palvella or “the Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapies to treat patients suffering from serious, rare skin diseases and vascular malformations for which there are no U.S. Food and Drug Administration (FDA)-approved therapies, today an...
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/20/3298897/0/en/Palvella-Therapeutics-Presents-New-SELVA-and-TOIVA-Data-at-the-2026-International-Society-for-the-Study-of-Vascular-Anomalies-World-Congress-Supporting-QTORIN-Rapamycin-as-a-Potent.html">Palvella Therapeutics Presents New SELVA and TOIVA Data at the 2026 International Society for the Study of Vascular Anomalies World Congress Supporting QTORIN™ Rapamycin as a Potential First-in-Disease Therapy for Multiple Serious, Rare Vascular Malformations</a>
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        In SELVA Phase 3 study, 100% of participants (13/13) aged 6–11 years were rated as “Much Improved” (+2) or “Very Much Improved” (+3) on the Microcystic Lymphatic Malformation Investigator Global Assessment (mLM-IGA) scale at Week 24, with a mean improvement of +2.46 (p
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/15/3295760/0/en/palvella-therapeutics-announces-new-data-from-the-phase-2-toiva-trial-of-qtorin-rapamycin-in-cutaneous-venous-malformations-presented-at-the-83rd-annual-meeting-of-the-society-for-.html">Palvella Therapeutics Announces New Data from the Phase 2 TOIVA Trial of QTORIN™ Rapamycin in Cutaneous Venous Malformations Presented at the 83rd Annual Meeting of the Society for Investigative Dermatology</a>
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        100% of patients with bleeding at baseline demonstrated a statistically significant improvement on the Cutaneous Venous Malformations Investigator Global Assessment Bleeding scale (cVM-IGA Bleeding) at Week 12 (+2.5 point improvement; p=0.003) 100% of patients with bleeding at baseline reported being &quot;satisfied&quot; or &quot;very satisfied&quot; with QTORIN™ rapamycin on the overall satisfaction item of the ...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/13/3293886/0/en/Palvella-Therapeutics-Announces-Uplisting-to-the-Nasdaq-Global-Market.html">Palvella Therapeutics Announces Uplisting to the Nasdaq Global Market</a>
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        Uplisting reflects Palvella&#39;s continued progress advancing potential first-in-disease therapies for serious, rare skin diseases and vascular malformations
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      <a target="_blank" rel="nofollow" href="https://www.marketbeat.com/instant-alerts/palvella-therapeutics-q1-earnings-call-highlights-2026-05-08/?utm_source=snapi">Palvella Therapeutics Q1 Earnings Call Highlights</a>
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        Palvella Therapeutics NASDAQ: PVLA said it remains on track to submit a New Drug Application in the second half of 2026 for QTORIN rapamycin in Microcystic Lymphatic Malformations, after reporting what executives described as positive Phase 3 results and outlining an expanded commercial plan supported by a recent $230 million financing.
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